Successful Liver Transplantation of Recurrent Fibrolamellar Carcinoma following Clinical and Pathologic Complete Response to Triple Immunochemotherapy: A Case Report.


Journal

Oncology research and treatment
ISSN: 2296-5262
Titre abrégé: Oncol Res Treat
Pays: Switzerland
ID NLM: 101627692

Informations de publication

Date de publication:
2022
Historique:
received: 04 04 2022
accepted: 01 05 2022
pubmed: 11 5 2022
medline: 9 8 2022
entrez: 10 5 2022
Statut: ppublish

Résumé

Fibrolamellar carcinoma (FLC) is a rare liver cancer that predominantly affects younger patients without a history of liver disease. Surgical resection is the cornerstone of therapy and represents the best potentially curative treatment option. Modest objective responses with cytotoxic chemotherapy alone or combined with immune checkpoint inhibitors (ICIs) have been reported; however, there are no established systemic therapy regimens for unresectable or metastatic FLC. We report a case of a 23-year-old woman with FLC who presented with a 11.5 × 8.3 cm left liver mass and subsequently underwent resection as initial therapy. Molecular analysis of her surgical tissue revealed a DNAJB1-PRKACA fusion gene. The patient developed biopsy-proven recurrent FLC with multiple liver lesions but without any distant metastatic disease only 3 months after initial resection. In light of emerging data, the patient was treated with a novel triple therapy regimen including 5-fluorouracil (5-FU), interferon (IFN) alfa-2b, and nivolumab. Partial radiographic response was achieved after 4 treatments and complete response was achieved after 12 cycles with the combination. The patient received 2 more doses of 5-FU/IFN alfa-2b without nivolumab and underwent orthotopic liver transplantation (OLT) 6 months after the last dose of ICI. Pathological examination of the explanted liver remarkably confirmed pathologic complete response. She remains recurrence-free and is on active surveillance. For patients with unresectable/recurrent FLC with no distant disease, the combination of 5-FU, IFN alfa-2b, and nivolumab could be an effective systemic therapy option. The use of this chemoimmunotherapy regimen to downstage FLC prior to OLT may be worth investigating further.

Identifiants

pubmed: 35537414
pii: 000524872
doi: 10.1159/000524872
doi:

Substances chimiques

DNAJB1 protein, human 0
HSP40 Heat-Shock Proteins 0
Nivolumab 31YO63LBSN
Fluorouracil U3P01618RT

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

430-437

Informations de copyright

© 2022 S. Karger AG, Basel.

Auteurs

Sandra Kang (S)

Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA, smkang3@emory.edu.

Joseph Magliocca (J)

Division of Transplantation, Department of Surgery, Emory University School of Medicine, Atlanta, Georgia, USA.

Marty Sellers (M)

Division of Transplantation, Department of Surgery, Emory University School of Medicine, Atlanta, Georgia, USA.

Giorgio Roccaro (G)

Division of Transplantation, Department of Surgery, Emory University School of Medicine, Atlanta, Georgia, USA.
Division of Digestive Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.

Wei Zheng (W)

Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.

Melina Pectasides (M)

Department of Radiology and Imaging Services, Emory University School of Medicine, Atlanta, Georgia, USA.

Amber Draper (A)

Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

Jessica Guadagno (J)

Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

Bassel El-Rayes (B)

Division of Hematology and Oncology, Department of Internal Medicine, O Neal Comprehensive Cancer Center, University of Alabama at Birmingham Heersink School of Medicine, Birmingham, Alabama, USA.

Mehmet Akce (M)

Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.

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Classifications MeSH